Canonical Allele Identifier: CA2374743056

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350600A= , CM000682.2:g.63350600A=	GRCh38
NC_000020.10:g.61981952A= , CM000682.1:g.61981952A=	GRCh37
NC_000020.9:g.61452396A=	NCBI36
NG_011931.1:g.15744T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.811T= MANE Select	ENSP00000359285.4:p.Cys271=
ENST00000370263.8:c.811T=	ENSP00000359285.4:p.Cys271=
ENST00000463705.5:n.1459T=
ENST00000467563.3:n.881T=
ENST00000498043.6:c.835T=
ENST00000615287.4:c.598T=	ENSP00000483388.1:p.Cys200=
ENST00000627000.1:c.*500T=	ENSP00000486914.1:n.*500T=
ENST00000630240.1:n.532T=
NM_000744.6:c.811T=	NP_000735.1:p.Cys271=
NM_001256573.1:c.283T=	NP_001243502.1:p.Cys95=
NR_046317.1:n.1067T=
XM_011528524.1:c.598T=	XP_011526826.1:p.Cys200=
XM_017027625.2:c.283T=	XP_016883114.1:p.Cys95=
XM_024451822.1:c.283T=	XP_024307590.1:p.Cys95=
NM_001256573.2:c.283T=	NP_001243502.1:p.Cys95=
NR_046317.2:n.1020T=
NM_000744.7:c.811T= MANE Select	NP_000735.1:p.Cys271=